Aminophylline (Hospira, Inc.)
Welcome to the PulseAid listing for the Aminophylline drug offered from Hospira, Inc.. This Methylxanthine [EPC],Xanthines [Chemical/Ingredient] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Hospira, Inc. |
| NON-PROPRIETARY NAME: | Aminophylline |
| SUBSTANCE NAME: | AMINOPHYLLINE DIHYDRATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Methylxanthine [EPC],Xanthines [Chemical/Ingredient] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2005-05-10 |
| END MARKETING DATE: | 0000-00-00 |
Aminophylline HUMAN PRESCRIPTION DRUG Details:
| Item Description | Aminophylline from Hospira, Inc. |
| LABELER NAME: | Hospira, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 25(mg/mL) |
| START MARKETING DATE: | 2005-05-10 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0409-5921_648b64fc-7de8-4fbc-a931-9794b035bb61 |
| PRODUCT NDC: | 0409-5921 |
| APPLICATION NUMBER: | ANDA087242 |
Other AMINOPHYLLINE DIHYDRATE Pharmaceutical Manufacturers / Labelers:
